iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs16719	in-del	-/AG	0.4711	0.116682	utr-variant-3-prime, nc-transcript-variant	KLHL32	GRCh38.p7	6:97140233	AATAAGACATCTGAG[-/AG]TTACTTGAGGCAAGT	114792
rs25637	in-del	-/AACA	0.496842	0.0396107	intron-variant	KLHL32	GRCh38.p7	6:97115992	TGAGGACAGCAGAAG[-/AACA]AACAGTCAAAGTCCA	114792
rs706990	snp	A/C	0.321771	0.240672	intron-variant	KLHL32	GRCh38.p7	6:96917619	TTGAAGTTCCTGCTG[A/C]GACCCTTGCAATATT	114792
rs734667	snp	C/G	0.232651	0.249397	intron-variant	KLHL32	GRCh38.p7	6:96961625	ATCTCAGATCTACCT[C/G]TCTGAAAATAGGGCT	114792
rs734836	snp	G/T	0.448912	0.167697	intron-variant	KLHL32	GRCh38.p7	6:97103277	GGAGTGCAGTGGTGC[G/T]ATCTCAGCTCACTGC	114792
rs736450	snp	A/T	0.212122	0.247114	intron-variant	KLHL32	GRCh38.p7	6:97027878	TCCAGTAGGAGACTC[A/T]AGAGCTGTTACTGTA	114792
rs736585	snp	C/T	0	0	intron-variant	KLHL32	GRCh38.p7	6:97077381	TAATGTGAATTCATT[C/T]GATAATGTCTGATTT	114792
rs756495	snp	A/G	0	0	intron-variant	KLHL32	GRCh38.p7	6:96943479	TTACTGCTGACCCCC[A/G]ATGTTGGATAACTTC	114792
rs756496	snp	A/G	0	0	intron-variant	KLHL32	GRCh38.p7	6:96943552	ccacattttgtatga[A/G]aaagcagaagcccag	114792
rs760829	snp	A/G	0.449345	0.150869	intron-variant	KLHL32	GRCh38.p7	6:97102538	TCATTTTATTTAGAA[A/G]TCTCATGTCATCAAT	114792
rs760830	snp	C/G	0.307671	0.243257	intron-variant	KLHL32	GRCh38.p7	6:97096222	TCTGAGCCAACAGCC[C/G]TCCTGTCCTCTGTCA	114792
rs760831	snp	C/T	0.484279	0.0872533	intron-variant	KLHL32	GRCh38.p7	6:97133255	AATAGCCCTGGTGCA[C/T]CAGCATATGAGCAGC	114792
rs761127	snp	C/T	0.213635	0.247341	intron-variant	KLHL32	GRCh38.p7	6:97017659	GAGATGGCCAGCCAA[C/T]TTAGGTTTCTCTTTT	114792
rs761128	snp	A/G	0.212122	0.247114	intron-variant	KLHL32	GRCh38.p7	6:96950991	AATACAAATTACTCA[A/G]TTTGAACAAAAAAAA	114792
rs761129	snp	C/G	0.424814	0.178718	intron-variant	KLHL32	GRCh38.p7	6:96992474	ctcttctctctctga[C/G]agcaatgcgcactag	114792
rs850575	snp	C/T	0.495135	0.0490805	intron-variant	KLHL32	GRCh38.p7	6:96916603	ggtcaaactgcttca[C/T]tggttcttccattct	114792
rs850576	snp	C/T	0.495135	0.0490805	intron-variant	KLHL32	GRCh38.p7	6:96916673	taacacaaaaatttt[C/T]gtatgtcttttcttc	114792
rs850577	snp	A/C	0.39709	0.20215	intron-variant	KLHL32	GRCh38.p7	6:96917363	CCCTGGAGACTCATA[A/C]CCTGTAGTCCTCAGA	114792
rs850578	snp	G/T	0.397813	0.201621	intron-variant	KLHL32	GRCh38.p7	6:96918289	ATAAAATTTGGGGAA[G/T]TCAGGGATGCTAGTT	114792
rs850579	snp	A/G	0.495135	0.0490805	intron-variant	KLHL32	GRCh38.p7	6:96919065	TCAGCACAGTGAGAG[A/G]TTCATGACCTAGACT	114792
rs850580	snp	A/T	0.418814	0.184396	intron-variant	KLHL32	GRCh38.p7	6:96921252	AGCTCCCATCATGTG[A/T]CTAGTTGATTATGTT	114792
rs850581	snp	C/T	0.494896	0.0502606	intron-variant	KLHL32	GRCh38.p7	6:96921780	TTCAAATCTGATTCT[C/T]CCAGAGCTGTTAGAA	114792
rs850582	snp	A/T	0.135484	0.22223	intron-variant	KLHL32	GRCh38.p7	6:96921883	TGATAGATGAAAAAA[A/T]TGCTGCAGAAACTTG	114792
rs850583	snp	C/T	0.49533	0.0480965	intron-variant	KLHL32	GRCh38.p7	6:96922318	ATATCAGGACAGGAA[C/T]GTTATGAGATGGTGT	114792
rs850584	snp	A/G	0.49533	0.0480965	upstream-variant-2KB, intron-variant	KLHL32	GRCh38.p7	6:96922668	TACTTCCCAAAAGCT[A/G]TTTTTTGGAATACTT	114792
rs850585	snp	A/G	0.495291	0.0482933	upstream-variant-2KB, intron-variant	KLHL32	GRCh38.p7	6:96923550	GTTTGCTCCCTCTGG[A/G]GGTTATCTGTCTGGC	114792
rs850586	snp	A/G	0.135143	0.222054	upstream-variant-2KB, intron-variant	KLHL32	GRCh38.p7	6:96923736	GATTTAACTTACTGC[A/G]AAGATAGTATGTTAA	114792
rs850587	snp	A/T	0.494976	0.0498674	upstream-variant-2KB, intron-variant	KLHL32	GRCh38.p7	6:96923947	GGGCCTGGCACACTC[A/T]AGTGCCACTTCCGAG	114792
rs864796	snp	C/T	0.321053	0.23969	intron-variant	KLHL32	GRCh38.p7	6:96926984	TCACAATGATGGATG[C/T]ATTTTTTCACATCAG	114792
rs879382	snp	A/C	0.189576	0.242588	intron-variant	KLHL32	GRCh38.p7	6:97088457	TTCATTTCAGTAGGG[A/C]CCTGTTAAATATCTT	114792
rs879383	snp	A/G	0.189261	0.242509	intron-variant	KLHL32	GRCh38.p7	6:97089591	GGGTTTCACTATGTT[A/G]GGCAGGCTGGTTTCA	114792
rs879384	snp	C/T	0.439363	0.163222	intron-variant	KLHL32	GRCh38.p7	6:97089124	AGAGGGAAATGGAGT[C/T]GGCAGATCTGTCCTC	114792
rs926553	snp	C/G	0.401215	0.199083	intron-variant	KLHL32	GRCh38.p7	6:97061585	AGGTGGTCCTTGAGT[C/G]ACCCTTCTTCCTATC	114792
rs932854	snp	A/G	0.417196	0.185864	intron-variant	KLHL32	GRCh38.p7	6:96915068	AAAAAGAAAGAATAA[A/G]TGTCACTTGTGCCTC	114792
rs946116	snp	A/G	0.22263	0.248497	intron-variant	KLHL32	GRCh38.p7	6:97045939	TATGAGAAAAAGAAA[A/G]CCAAATGAGATGAAA	114792
rs946117	snp	A/G	0.150333	0.229274	intron-variant	KLHL32	GRCh38.p7	6:97061288	TCACTGGGGGTAGAG[A/G]CAATGCCCAACCTAG	114792
rs946118	snp	C/G	0.152667	0.230274	intron-variant	KLHL32	GRCh38.p7	6:97065132	TTTCAGTAACAGTAT[C/G]TAGTAAATCACAAAG	114792
rs946119	snp	C/T	0.152667	0.230274	intron-variant	KLHL32	GRCh38.p7	6:97065215	GGGATGAGTAATGTG[C/T]GTATTCCTCCCTGAT	114792
rs946120	snp	A/G	0.499859	0.0083854	intron-variant	KLHL32	GRCh38.p7	6:97096453	CACCACTCCAAGCGT[A/G]TATATTCCATTCATC	114792
rs946121	snp	A/G	0.103082	0.202275	intron-variant	KLHL32	GRCh38.p7	6:97026104	atacattatatatat[A/G]taaatGTTCATAGGA	114792
rs963402	snp	A/G	0.147656	0.228091	intron-variant	KLHL32	GRCh38.p7	6:97080449	TCCCTACTGGATACC[A/G]GGGACACACAAGGCA	114792
rs974417	snp	A/G	0.384593	0.210677	intron-variant	KLHL32	GRCh38.p7	6:96971722	TTCCACCTGAACACT[A/G]TAACGGCTTTAGGCA	114792
rs976901	snp	A/G	0.00953873	0.0683987	intron-variant	KLHL32	GRCh38.p7	6:96909244	CACATGGAAGTGAGG[A/G]TGGTAGAGATAGACA	114792
rs982124	snp	C/T	0.0966517	0.197444	intron-variant	KLHL32	GRCh38.p7	6:96933982	AATTTATACAGGAGA[C/T]TTAGGCACAGAGTTC	114792
rs985481	snp	C/T	0.123105	0.215401	upstream-variant-2KB	KLHL32, NDUFAF4	GRCh38.p7	6:96898025	CGCCGGAAGCGGCCC[C/T]CGTGGGAGCCGTCAC	114792
rs998195	snp	A/C	0.45235	0.146814	intron-variant	KLHL32	GRCh38.p7	6:97077520	ATATAGAAAACAAGG[A/C]GACCCAAGATTCACT	114792
rs998196	snp	A/C	0.00557542	0.0525036	intron-variant	KLHL32	GRCh38.p7	6:97077606	CCAATTGTATGAAAA[A/C]CCCAGTACCTAGATA	114792
rs1028878	snp	G/T	0.420639	0.182709	utr-variant-5-prime, upstream-variant-2KB	KLHL32, NDUFAF4	GRCh38.p7	6:96898701	TTTGTTTGTTTGTTT[G/T]TTTTTTCTGACGTCT	114792
rs1119219	snp	G/T			intron-variant	KLHL32	GRCh38.p7	6:97003996	atgaattttaaaata[G/T]ttatttctaattctg	114792
rs1119220	snp	A/G	0.461148	0.133852	intron-variant	KLHL32	GRCh38.p7	6:97004035	gctattggttgtttt[A/G]taggaatagcactga	114792
rs1119221	snp	A/G	0.461037	0.134028	intron-variant	KLHL32	GRCh38.p7	6:97004111	tcttcctattcatga[A/G]tatggaatgtttttc	114792
rs1206077	snp	A/C	0.142609	0.225759	intron-variant	KLHL32	GRCh38.p7	6:96914889	gaacttagtgcagac[A/C]cccaatcagcgtagc	114792
rs1206078	snp	A/G	0.420574	0.182769	intron-variant	KLHL32	GRCh38.p7	6:96915413	GACACTGACATATGA[A/G]CAAAAAATTTCAGTA	114792
rs1206079	snp	C/G	0.397271	0.202018	intron-variant	KLHL32	GRCh38.p7	6:96915901	gcaggacataaattt[C/G]cctttataaaggtgc	114792
rs1206080	snp	A/T	0.495095	0.0492773	intron-variant	KLHL32	GRCh38.p7	6:96915908	ataaatttcccttta[A/T]aaaggtgctcccctt	114792
rs1206084	snp	A/G	0.321292	0.23962	intron-variant	KLHL32	GRCh38.p7	6:96925709	CCAGAACAGGAATAC[A/G]TTTGTGAATTCGTAA	114792
rs1206087	snp	A/G	0.125182	0.216612	intron-variant	KLHL32	GRCh38.p7	6:96999905	GTTGCAAGGGCTCCT[A/G]AAACATCACCACTAC	114792
rs1206088	snp	C/T	0.105569	0.204058	intron-variant	KLHL32	GRCh38.p7	6:97001292	atgtggaactctcta[C/T]actttctactcagtt	114792
rs1206089	snp	C/T	0.498009	0.0314867	intron-variant	KLHL32	GRCh38.p7	6:97004867	gatgtgctgctgggt[C/T]tggtttattagtatt	114792
rs1206090	snp	A/G	0.498009	0.0314867	intron-variant	KLHL32	GRCh38.p7	6:97005569	tcttctaggtgtgat[A/G]ttaggttgttaattt	114792
rs1206091	snp	A/G	0.498009	0.0314867	intron-variant	KLHL32	GRCh38.p7	6:97006241	cttttcattgagtga[A/G]tccttcaccattagg	114792
rs1206092	snp	C/T	0.105214	0.203807	intron-variant	KLHL32	GRCh38.p7	6:97006700	tgtggtaatgaattc[C/T]tgtaccatttgcttg	114792
rs1206093	snp	C/T	0.118933	0.212888	intron-variant, upstream-variant-2KB	KLHL32	GRCh38.p7	6:97008533	actcccatgccaaac[C/T]ctctgagctgtgcac	114792
rs1206094	snp	C/T	0.497984	0.0316851	intron-variant	KLHL32	GRCh38.p7	6:97012205	ccaaagatgtccatg[C/T]cctaatttctggagc	114792
rs1206095	snp	A/T	0.124837	0.216412	intron-variant	KLHL32	GRCh38.p7	6:97013075	ATGTAATTTTGTGAG[A/T]AAAGGATACTTACCC	114792
rs1206096	snp	A/T	0.497829	0.0328757	intron-variant	KLHL32	GRCh38.p7	6:97014074	CACTTTGGGAGGCCG[A/T]GGCGGGCGGATCACG	114792
rs1206097	snp	A/G	0.123452	0.215605	intron-variant	KLHL32	GRCh38.p7	6:97018780	atgctggccaaagta[A/G]caatctatcagatga	114792
rs1206098	snp	A/G/T	0.454511	0.231988	intron-variant	KLHL32	GRCh38.p7	6:97019937	ggcgcccatcaccac[A/G/T]cccggcgaatttttt	114792
rs1206099	snp	G/T	0.124837	0.216412	intron-variant	KLHL32	GRCh38.p7	6:97020337	TAAAAAATGAAAAAA[G/T]GTGTTATCTAGAGAT	114792
rs1206100	snp	A/G	0.414905	0.187899	intron-variant	KLHL32	GRCh38.p7	6:97021514	ctattcaggctttca[A/G]ttgactagatgagtc	114792
rs1206101	snp	C/G	0.14665	0.227637	intron-variant	KLHL32	GRCh38.p7	6:97026953	tggatcatgaggtca[C/G]gaattcgagaccagc	114792
rs1206102	snp	C/T	0.273587	0.248885	intron-variant	KLHL32	GRCh38.p7	6:97029905	CCATTGTAAACATCA[C/T]TAATTATGTAACAGT	114792
rs1206103	snp	A/T	0.273587	0.248885	intron-variant	KLHL32	GRCh38.p7	6:97030143	TTTGCCTGTGTTCAG[A/T]GTAACTCCAAAGCTG	114792
rs1206104	snp	A/G	0.273856	0.248859	intron-variant	KLHL32	GRCh38.p7	6:97031298	TTTTTTAATCTTTAG[A/G]TTAGTTCTAGTTTTT	114792
rs1206105	snp	C/T	0.273587	0.248885	intron-variant	KLHL32	GRCh38.p7	6:97031583	cctcaagtgaacttc[C/T]agcctcagcctccca	114792
rs1206106	snp	A/T	0.407502	0.194147	intron-variant	KLHL32	GRCh38.p7	6:97031616	GTGGTGGGATTATAG[A/T]CATGACCCACGGTGC	114792
rs1206107	snp	A/G	0.273587	0.248885	intron-variant	KLHL32	GRCh38.p7	6:97031780	TAAAGTCCTGAAGCC[A/G]GAGATAGGGATTTAG	114792
rs1206108	snp	A/G	0.40263	0.198	intron-variant	KLHL32	GRCh38.p7	6:96990874	taggtaaagcactta[A/G]ggtctttgttccttc	114792
rs1206109	snp	A/G	0.404733	0.196361	intron-variant	KLHL32	GRCh38.p7	6:96990991	aatcacagacccgtt[A/G]ctaatgggaatgttt	114792
rs1206110	snp	C/G	0.403684	0.197183	intron-variant	KLHL32	GRCh38.p7	6:96991105	ctcctctccttatgg[C/G]ggttttggtgctggg	114792
rs1206111	snp	A/G	0.498059	0.0310896	intron-variant	KLHL32	GRCh38.p7	6:96992712	TGCCCCTCATACTCT[A/G]ATAGGTTATGCACAA	114792
rs1206112	snp	C/T	0.497907	0.0322805	intron-variant	KLHL32	GRCh38.p7	6:96993679	tgcaagctaactagt[C/T]aggctaccacactgt	114792
rs1206113	snp	C/T	0.125182	0.216612	intron-variant	KLHL32	GRCh38.p7	6:96994836	ACAGTCAGACCAGGA[C/T]TTCTTTCATCAAAGT	114792
rs1206114	snp	A/G	0.497933	0.032082	intron-variant, upstream-variant-2KB	KLHL32	GRCh38.p7	6:96998431	TCTTTTTCAGAAAAA[A/G]AATTAATAAAAATAA	114792
rs1206115	snp	C/T	0.124837	0.216412	intron-variant, upstream-variant-2KB	KLHL32	GRCh38.p7	6:96998577	CCTGCAGTTGTCTAA[C/T]TGGTGCATGAATGTC	114792
rs1206116	snp	A/G	0.358728	0.225118	intron-variant	KLHL32	GRCh38.p7	6:97057494	gccgagtatcttttt[A/G]tatgcttatttgcca	114792
rs1206117	snp	A/G	0.401215	0.199083	intron-variant	KLHL32	GRCh38.p7	6:97060236	TGATCACAGGCAGGA[A/G]AAAAAAAAAGGTCAC	114792
rs1206118	snp	C/T	0.152667	0.230274	intron-variant	KLHL32	GRCh38.p7	6:97061105	GAACAGCCCCTTGTG[C/T]TCCACCACCTGGAGG	114792
rs1206130	snp	A/T	0.192715	0.243348	intron-variant	KLHL32	GRCh38.p7	6:97092371	CATAATATCTCCTAT[A/T]TTTTAAAGTTACCAT	114792
rs1206131	snp	C/T	0.193028	0.243422	intron-variant	KLHL32	GRCh38.p7	6:97093132	GTAGAATATTACTTA[C/T]GCATTGGTGCCCTGC	114792
rs1206132	snp	A/G	0.148326	0.228391	intron-variant	KLHL32	GRCh38.p7	6:97093449	CACAGTATAGATTTC[A/G]ATGGAGGTCTCACTG	114792
rs1206133	snp	C/T	0.40733	0.194287	intron-variant	KLHL32	GRCh38.p7	6:97095261	CTGTAATCAATTTCT[C/T]ATTCTGCCCACTGCT	114792
rs1206142	snp	C/T	0.484632	0.086302	intron-variant	KLHL32	GRCh38.p7	6:97134125	ATAATAAAAACAATA[C/T]ACAGCAAAGCTTGTG	114792
rs1206143	snp	C/T	0.484491	0.0866827	intron-variant	KLHL32	GRCh38.p7	6:97135753	TTACAGGCTATATTA[C/T]CATTCATTCTGAACT	114792
rs1206144	snp	A/G	0.492286	0.0673169	intron-variant	KLHL32	GRCh38.p7	6:97136066	TAAATTTTTTGTGTC[A/G]TCAGTCACAAATCTG	114792
rs1206145	snp	C/G	0.498813	0.0243321	intron-variant	KLHL32	GRCh38.p7	6:97137910	AGATCATTAAAGACG[C/G]GTACAAAGAGGTCTG	114792
rs1206146	snp	C/T	0.496874	0.0394129	intron-variant	KLHL32	GRCh38.p7	6:97115346	TTGTTTTTAATTATC[C/T]GTGAATGGTAGTTAC	114792
rs1206147	snp	A/G	0.496681	0.0405994	intron-variant	KLHL32	GRCh38.p7	6:97117297	AATTTAATTGATGGG[A/G]ATTGAATCATTGGCA	114792
rs1206148	snp	C/T	0.496842	0.0396107	intron-variant	KLHL32	GRCh38.p7	6:97118588	CACACCACTGCACTC[C/T]AGCCTGGGCAAGAAA	114792
rs1206149	snp	A/G	0.464841	0.127841	intron-variant	KLHL32	GRCh38.p7	6:97119062	CACTTGAACTTCATG[A/G]TCCAATCACTTCAAT	114792

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